ADAPT JOINS COALITION IN SUPPORT OF BUILD BACK BETTER
Disability Connection Midsouth builds on the blog from the Memphis Center for Independent Living to keep up with issues that impact the disability community and the midsouth. Please respond and add your voice to be a part of the discussion about important topics in the Memphis area and things that impact people with disabilities nationwide.
Friday, December 10, 2021
ADAPT Supports Build Back Better
Wednesday, October 27, 2021
Help Make Voting Accessible
NIST Seeks Public Comment on Recommendations for Promoting Access to Voting for People with Disabilities
The National Institute of Standards and Technology (NIST) requests public comments on the Draft of Promoting Access to Voting: Recommendations for Addressing Barriers to Private and Independent Voting for People with Disabilities. Under Executive Order 14019 on Promoting Access to Voting, NIST is directed to identify barriers to private and independent voting for people with disabilities, make recommendations to remove these barriers, and evaluate the steps needed to ensure that the online Federal Voter Registration Form is accessible to people with disabilities. The Draft is available in the Federal Register.
The Draft was developed by NIST using information collected through the Request for Information that was published in the Federal Register on June 16, 2021, reviews of reports, papers and other literature, and engagement with stakeholder organizations and election officials. NIST is seeking comment on the Draft from persons with disabilities, disability advocacy groups, assistive technology vendors and professionals, non-partisan voting promotion groups, voting technology vendors, election officials, and other stakeholders.
Public comments must be received by 5:00 pm ET on November 22, 2021. Comments may be submitted at www.regulations.gov under NIST-2021-0005-0001 or by email at pva-eo@list.nist.gov. Complete instructions for comment submission can be found in the Federal Register notice. For questions about this request for public comment, contact Kevin Mangold, NIST, by phone at 1-301-975-5628 or email Kevin.Mangold@nist.gov. Users of telecommunication devices for the deaf, or a text telephone, may call the Federal Relay Service at 1-800-877-8339.
Monday, October 11, 2021
International Day of the Girl
Friends,
Today is International Day of the Girl. It’s a day to celebrate our strides towards equity and re-commit our focus, so we can continue to elevate our programs and partnerships as, together, we lift up all girls, everywhere, to reach their potential.
For Nike, focusing on play isn’t anything new. We’re doubling down on the future of play for kids across the company. But in the last few years, we’ve deepened our focus on girls, establishing programs and targets geared at moving further, even faster. The simple reality is that girls experience complex cultural, social and economic barriers to play and sport. And as a result, they lack the support of caring, trained coaches who look like them, and access to the right product to play.
To meet these challenges head on, over the past two years we’ve donated 75,000 Nike sports bras and 3,000 Nike Pro Hijabs through our community and business partners to girls around the world, so they have what they need to successfully, and confidently, participate in sport. To enhance the experience for girls, we’ve also built tools for caring adults to guide conversations, and fit cards for girls so they can determine for themselves how these products should feel, and fit, to support their sport journey. And in the spirit of open-source innovation, we’re sharing our sports bra and hijab playbooks – with everyone.
We’ve also developed specific tools for how caring adults can step up and learn how to coach girls. The Coaching Girls Guide – another tool free to anyone, created in partnership with We Coach (now the Center for Healing and Justice Through Sport), with additional support from Youth Sport Trust in Europe, the Middle East and Africa – equips coaches with tools to connect with girls to help make sport fun.
For IDOTG, our Kids team has re-imagined the guide and brought it front-and-center for the empowering adults in kids’ lives. On @NikeWomen Instagram, our new film puts girls at the center to answer questions as only kids can and make spirited statements about what play and sport looks like for them – and what they need from us to keep showing up as they play bold, brave and new.
All around the world, in the key cities and employee backyards where we partner with nonprofit organizations to create active, inclusive communities, we’re upping the ante for girls so they’re getting the same opportunities to play – and stay playing – for a lifetime. More than 135 partners spanning six continents have our support, and investment, for the on-the-ground programming necessary to level the playing field.
We hope you’ll celebrate with us:
- Join us today on social media to share how you’re empowering and advocating for girls in sport.
- Take action by reading the five facets of creating girl-friendly play and sport environments.
- Participate in an ICOACHKIDS-hosted webinar about motivating girls to stay active on Oct. 14 at 2 p.m. CET in partnership with Youth Sport Trust International, TAFISA and Nike.
- Learn how Naomi Osaka’s Play Academy is extending its investment to nonprofits supporting girls in LA and Tokyo to join our Haiti partner.
- Get ready to cheer on the Angel City Football Club as they announce a significant donation of Nike sports bras to LA-area nonprofits.
Because when it comes to getting more girls connected to the power of play and sport, the ball is in all our courts – today, on IDOTG, and the 364 days in between. My sincere thanks for teaming up with us to make sure we keep that ball, and all girls, moving.
Forward,
Caitlin Morris
Vice President of Social & Community Impact, NIKE, Inc.
@Cmorris_nike #MadeToPlay
Thursday, October 7, 2021
Disability Rights, Care Workers To Hold 24-Hour Vigil at the U.S. Capitol To Hold the Line on Care Funding
/in Advocacy, From the Frontlines, News, Press Releases, Public Policy/by Pam KatzAs negotiations around the biggest jobs plan since the New Deal stall, care advocates from across the country will hold a 24-hour vigil outside the U.S. Capitol to urge elected leaders to hold the line on caregiving funding in the Build Back Better plan.
People with disabilities, direct care workers, older adults, and caregivers will share the steep health and financial costs that families pay as a result of poverty wages paid to care workers and long waitlists for home and community-based services (HCBS). Advocates traveling from states hard hit by COVID-19—including Tennessee, Texas and Kansas—will continuously read stories collected from thousands of impacted individuals—disproportionately people of color— across the country who aren’t able to travel to D.C. in part because they don’t have the paid leave, child care or long-term services that enable them to do so. Overwhelming majorities of people across the country want Congress to invest in long-term care and support the Build Back Better’s plan to do so.
WHAT:
A 24-hour vigil in front of the Capitol during which advocates will continuously read stories of those struggling to access home and community based services and to make enough money to care for themselves and their families. The vigil will culminate in a closing ceremony with advocates delivering boxes of printed out stories to members of Congress.
The event is co-hosted by ACLU, ADAPT, The Arc of the United States, Autistic Self Advocacy Network, AAPD, Bazelon Center for Mental Health Law, Be A Hero, Care Can’t Wait Coalition, Caring Across Generations, Little Lobbyists, Justice in Aging, National Council on Independent Living, National Domestic Workers Alliance, National Council on Aging, National Health Law Program, and SEIU.
WHEN:
Vigil: Wed, Oct 6 at 7 pm to Thurs, Oct 7 at 7 pm
Closing Program: Thurs, Oct 7 from 6-7 pm
WHERE:
Union Square in front of Capitol Reflecting Pool
The area is bounded by Pennsylvania Avenue, NW; First Street, NW/SW; Maryland Avenue, SW; and Third Street, SW/NW
Live Stream: https://fb.me/e/3WaL3atkg
WHO:
Closing ceremony speakers:
- Bob Casey, S. Senator representing Pennsylvania
- Maria Town, President and CEO, AAPD
- Mike Oxford, National Organizer, ADAPT
- Nicole Jorwic, Senior Executive Officer of State Advocacy and Public Policy, The Arc
- April Verrett, President of SEIU, Local 2015
Vigil speakers available for media interviews:
- Domonique Howell, a Black and disabled advocate from Philadelphia. She is an independent living specialist and co-chair of ADAPT’s housing work group.
- Latoya Maddox, a Philadelphia-based Black disabled mother who has used home and community-based services for the past 17 years
- Lydia Nunez, Ombudsman and organizer with Gulf Coast ADAPT in Texas. She is white and disabled and fights for home and community-based services for other people with disabilities and older adults.
- Josue Rodriguez, a Latino organizer with El Paso ADAPT who uses HCBS for attendant services.
- Family caregivers and care workers
VISUALS:
People holding posters and banners featuring portraits of care workers, family caregivers, aging adults and people with disabilities. Miniature houses featuring portraits of care recipients, caregivers and care workers
BACKGROUND:
More than 800,000 people with disabilities are on waiting lists for home and community-based services (HCBS), such as in-home care, meal delivery, transportation services and respite care. The Better Care Better Jobs Act—introduced in the Senate by lead sponsor Sen. Bob Casey and in the House by lead sponsor Rep. Debbie Dingell and supported by over 480 organizations—provides a blueprint for how $400 billion investment in HCBS could support a profoundly undervalued and underpaid workforce and get hundreds of thousands of people off waitlists by helping to:
- Increase access to HCBS: expanding financial eligibility criteria for HCBS and supports for family caregivers, and adopting programs that help people navigate enrollment and eligibility.
- Make permanent “Money Follows the Person,” a federal demonstration program that helps aging individuals and people with disabilities transition back to their homes and communities from institutions by providing federal matching funds that incentivizes HCBS in states
- Support oversight and monitoring of the quality of HCBS
- Increase HCBS payment rates to promote recruitment and retention of care workers
Wednesday, October 6, 2021
ADAPT Confronts #BuildBackBetter Holdouts
Disability Activists Confront #BuildBackBetter Holdout Senators
Who: National ADAPT
What: Confronting Democratic Senators blocking passage of the Build Back Better social infrastructure bill
Where: Outside Hart Senate Office Building at 120 Constitution Ave NE, Washington, DC 20002, Offices of Sen. Kyrsten Sinema and Sen. Joe Manchin
When: Happening Now, Wednesday, October 6, 2021
Why: To demand Sen. Sinema and Sen. Manchin stop blocking passage of the Build Back Better social infrastructure bill, and support full funding of Home and Community-Based Services (HCBS), which keeps people out of institutions. HCBS funding also provides living wages for the attendants who provide essential, often intimate care for older and disabled people. ADAPT is also demanding that both senators support funding for affordable, accessible, integrated housing, because you can’t have HCBS without the “H.”
ADAPT Demands Congress to Immediately Pass the Build Better Act with FULL funding for Home and Community Based Services and Housing Options
ADAPT has been urging Congress to Act of these critical issues for over 30 years. These programs enable people to live outside institutions and in freedom in their communities. Full Funding means the following:
- Expansion of HCBS under Medicaid, Medicare, and the Affordable
Care Act as a required service in all states (rather than a waiver-based
program) to increase access, quality, uniformity nationwide.
- Increase payment rates in a manner that will guarantee a “living
wage” and benefits to attendant care workers employed in home care.
- Expand affordable, accessible housing development and rent
subsidy programs targeting low and moderate income people with
disabilities, especially people who receive HCBS services.
- Expand access to accessible home modifications programs to enable people to leave or avoid institutional settings thus saving millions of health care dollars.
These priorities target people with low incomes and do not create new programs. It is time for Congress to keep its promise to ADAPT and Americans to invest in the long term care infrastructure.
NationalADAPT.org @RealNatlADAPT on Twitter & Instagram, ADAPT National on Facebook and TikTok, National ADAPT on YouTube ADAPTnational@gmail.com#DisabledNotDisposable #CareCantWait #BuildBackBetter #HoUSed #ADAPTandSurvive
In-Home Vaccination Program
Tennessee Home Vaccinations
The in-home Covid-19 vaccine program has undergone some changes due to some people having experienced long delays in getting the vaccine. Due to the changes, seniors over the age of 60 are no longer eligible for the program based on age alone.
The key program changes are:
- Seniors no longer qualify based on age alone. To qualify you must be a Tennessean with a disability over 18 or any family or caregiver in their household.
- The program is available in 87/95 counties. They don't have home health providers available in the Chattanooga area. However, they're working on it.
- Rather than the Tennessee Disability Coalition or our partners filling out online forms, everyone is referred to Disability Rights Tennessee's main intake number. They have staff trained and ready to connect folks.
- The Disability Rights Tennessee phone number is 1-800-342-1660. Hablamos Español.
No proof of disability or citizenship is needed. Callers’ information will only be used to schedule the vaccine appointment. Information will not be shared for any other reason.
Disability Rights Tennessee phone number is 1-800-342-1660. Hablamos Español.
Monday, August 23, 2021
Mask Accommodations and Alternatives
The Tennessee Disability Coalition Mask Accommodations and Alternatives:
The Tennessee Disability Coalition is pleased to share the following brief list of mask accommodations and alternatives. Each of us experience disability differently and most have become experts on how to accommodate our own individualized needs. If you have questions about what reasonable accommodation someone needs- start by asking them. If you would like to share an accommodation that works for you or a loved one, or talk about other options please contact us at: coalition@tndisability.org or 615-383-9442.
The Americans with Disabilities Act (ADA) and Face Mask Policies:
Southeast ADA Center facts, best practices and examples of reasonable accommodations: https://www.adasoutheast.org/ada/publications/legal/ada-and-face-mask-policies.php#t4a
Clear Masks:
Here are a few manufacturers of
clear masks. You can also find online directions for making them yourself.
- ClearMask
- Leaf Mask
- SafeNClear The Communicator mask
- Smile Masks
- Directions for making your own
mask with a clear window
- Badger Shield + face shield*
- Rapid Response PPE face shield*
*Note: “It is not known whether face
shields (a clear plastic barrier that covers the face) provide the same source
control for droplets as face masks, but they may be an option in situations
where wearing a face mask is problematic. For optimal protection, the shield
should extend below the chin and to the ears, and there should be no exposed
gap between the forehead and the shield's headpiece."
In Tennessee - Bridges has clear masks for sale. These can be ordered on their website using the following order form: https://www.bridgesfordeafandhh.org/masks-for-deaf-hard-of-hearing
Over-The-Head Hoodie Option:
Recommendations for Individuals with Autism and Those with Sensory Challenges:
Sensory-Friendly Masks: https://nationalautismresources.com/sensory-friendly-fabric-masks/
Wednesday, August 18, 2021
Pathfinder Website Upgrade
Tennessee website for finding disability services gets major upgrade
NASHVILLE
– An overhaul of
Tennessee Disability Pathfinder’s website makes it easier for people with
disabilities to find needed services. The statewide portal can now be found
more easily at TNPathfinder.org. Updated interactive features match
users anywhere in Tennessee with disability resources, service providers and community
events.
Tennessee Disability Pathfinder is a project of the Vanderbilt Kennedy
University Center for Excellence in Developmental Disabilities, part
of the Vanderbilt University Medical Center. It has been primarily funded by
the Tennessee Council on Developmental Disabilities, which also led funding for
the upgrade.
Pathfinder helps people
with disabilities, family members, caregivers, educators, and other
professionals find and access community resources, support, and services to
meet their needs. Users can get help through a toll-free helpline, online directory,
and regularly scheduled community workshops across Tennessee. Pathfinder’s
diverse staff can help people of all ages, types of disabilities, and languages
spoken.
Council on Developmental
Disabilities Executive Director Wanda Willis said, “This upgrade is a huge jump
forward. It just got easier to find the support people with disabilities in
Tennessee need to live great lives. I am especially proud of how many public
and private partners came together to make this happen.”
New
features of the Pathfinder website
More than 3,500
disability resources across Tennessee are accessible on the new website.
Searching for information has been made more customized. Users can search based
on:
- Stage of Life: Choose from Prenatal/Infancy, Early
Childhood, School Age, Transition/Young Adult, Adulthood, or Aging
- Topic of Interest: Twenty service categories to select,
with a text box to type keywords
- Diagnosis: Type of disability or health condition
- Benefit/Payment Options: Forms of payment accepted by the agency
provider, such as health insurance, government program, private pay, or no cost
- Service Area: Select counties where services are provided
Pathfinder’s website will still
be open for anyone to use without creating an account, but there will be new
features for users who choose to create a profile, like:
- the
ability to bookmark resources,
- save
past searches,
- submit
new agency resources and website links to be added to the site,
- and post events on the Pathfinder Events Calendar.
The new Pathfinder website
also includes new accessibility features. An accessibility menu provides tools
to adjust color contrast, magnification, and font styles. Users are also able
to translate the website into one of eight different languages.
A cross-state
partnership
The new Pathfinder website
is a collaboration with the AWS Foundation. The AWS
Foundation saw the need for a central website of disability-related information
in its home state of Indiana. After a nationwide search, Pathfinder’s online
directory was the model they chose to use. They created the Indiana
Disability Resource Finder (FINDER).
The AWS Foundation now
provides the new platform for Tennessee Disability Pathfinder. The platform was
designed by Aptera. A project team worked together to develop the Tennessee
Disability Pathfinder website and its new system.
“It has been a great
experience working with Vicki Johnson, AWS Director of System Navigation &
Marketing, the AWS Foundation, and Aptera,” said Pathfinder program director
Megan Hart. “This upgrade has allowed us to keep the important parts of
Pathfinder’s website while adding new features that allow users to better access
and save information.”
“Individuals with
disabilities, their families, community providers and others need quick and
easy access to information about supports and services across Tennessee. We’re
proud of the entire Pathfinder team and the Vanderbilt Kennedy Center’s
partnership with so many state agencies and the AWS Foundation and Aptera to
make this new website a reality,” said Elise McMillan, JD, Co-Director of the
Vanderbilt Kennedy University Center for Excellence in Disabilities and the Faculty
Director of Pathfinder.
Pathfinder
will celebrate the new website with an online launch celebration starting at
9:00 a.m. CT on Sept. 1 across its social media pages, complete with special guests, entertainment, and
giveaways. Follow them on Facebook (https://www.facebook.com/tnpathfinder),
Instagram (https://www.instagram.com/tnpathfinder/),
and Twitter (https://www.twitter.com/tnpathfinder)
to join in on the celebration.
New
Pathfinder funding partnerships
The new Tennessee
Disability Pathfinder website was also made possible through expanded funding
partners through the State of Tennessee. New partners include:
- Tennessee
Commission on Aging & Disability
- Tennessee
Department of Education
- Tennessee
Department of Mental Health & Substance Abuse Services
- Tennessee Department of Human Services, Division of Rehabilitation Services
These join existing
funding partners:
- Tennessee
Council on Developmental Disabilities
- Tennessee
Department of Health
- Tennessee
Department of Intellectual and Developmental Disabilities
Monday, August 16, 2021
TDH Offering Booster Vaccine
TENNESSEE DEPARTMENT OF HEALTH OFFERING THIRD DOSE OF mRNA VACCINE
- Received an organ transplant and are taking medicine to suppress the immune system • Received a stem cell transplant within the last 2 years or are taking medicine to suppress the immune system
- Moderate or severe primary immunodeficiency (such as DiGeorge syndrome, Wiskott-Aldrich syndrome)
- Advanced or untreated HIV infection
- Active treatment with high-dose corticosteroids or other drugs that may suppress your immune response For more information on the CDC’s recommendation for an additional dose of an mRNA COVID-19 vaccine is available online. A notification has been sent to all Tennessee providers with information on these recommendations. Providers are encouraged to begin offering the additional dose option 710 James Robertson Parkway
- Andrew Johnson Tower, 5th Floor Nashville, TN 37243
- tn.gov/health to eligible patients.
Friday, August 6, 2021
Institutionalization is a Public Health Crisis
In the face of the Delta variant, there is a critical course of action to take now: GET PEOPLE OUT!
By Bruce E. Darling
In March, the COVID Tracking Project at the Atlantic reported that about 8% of people who live in US long-term-care facilities had died of COVID-19 – nearly 1 in 12. However, in nursing facilities alone, the death toll jumped to nearly 1 in 10. As vaccinations began rolling out in nursing facilities, people expressed relief as the rate of institutional COVID deaths plummeted. With the sense that victory had been achieved, disability rights advocates began to pivot away from the current public health crisis and started talking about planning for “the next pandemic”.
Unfortunately, “the next pandemic” may already be here.
Last week, the Washington Post reported that “The war has changed” and released internal documents from the Centers for Disease Control, reporting that the Delta variant is “so contagious that it acts almost like a different novel virus, leaping from target to target more swiftly than Ebola or the common cold.” The new strain is now reported to be about as transmissible as chickenpox – with each infected person infecting as many as eight or nine others, on average.
The CDC document also indicated that Delta variant vaccine breakthrough cases may be as transmissible as unvaccinated cases, meaning that vaccinated individuals may become infected and then infect others. The CDC document highlighted that “vaccine breakthrough cases will occur more frequently in congregate settings, and in groups at risk of primary vaccine failure (i.e., immune compromised, elderly, etc.).” And finally, the CDC identified that the Delta variant may cause more severe disease than Alpha or other previous strains of the virus.
The implications for institutionalized individuals, particularly elderly and Disabled individuals in nursing facilities, are significant. First, according to the CDC, as of the middle of July, 18.7% of nursing facility residents and 41.4% of nursing facility staff still have NOT been vaccinated for COVID. That means tens of thousands of nursing facility residents are sitting ducks for the virus. But that doesn’t mean other nursing facility residents are safe. As the virus mutates, breakthrough infections have become more frequent and although vaccination still reduces the risk of serious illness, nursing facility residents are most at risk for that outcome. Additionally, because nursing facility residents were among the first to be vaccinated, it is likely that any waning of immunity will first appear in this group. We probably have already started to see this in clusters of nursing facility deaths that have begun to crop up across the country.
In the internal document secured by the Washington Post, the CDC recommended that given increased transmissibility, lower vaccine effectiveness, and current vaccine coverage, nonpharmaceutical interventions are needed to reduce transmission of the Delta variant. Most of these public health efforts will focus on preserving the health and safety of people in the community as a way to reduce the strain on healthcare systems, but such efforts – absent specific efforts to address the likely deaths in congregate settings are inherently ableist, particularly when demonstrated solutions exist to protect Disabled lives.
During the early months of the pandemic, research demonstrated that community integration of Disabled individuals reduced the spread and deaths from COVID-19. Research published in JAMDA, the Journal of Post-Acute and Long-Term Care Medicine, compared the infection and death rates of people in Connecticut nursing facilities to those receiving services in the community and demonstrated that people receiving services in the community were 11 times less likely to get infected with COVID-19 and die than their nursing facility counterparts.
Although people may assume that the COVID-19 deaths in nursing facilities and other institutions were unavoidable or exacerbated because people in institutions are “sick” and “frail,” the research told a different story. The researchers found that – after infection – the death rates in the community and in the nursing facilities were comparable which means the nursing facility residents were not, in fact, more “frail” than their peers in the community. In summarizing their findings, the researchers noted that “The main distinction between groups was their living situation. It is likely that living in the community, vs a congregate setting, accounts for the significantly lower infection rates.”
Public health efforts that ignore congregate settings are not just ableist, they are also racist. Incarcerated individuals – who are over represented by Black, Indigenous, and People of Color (BIPOC) – exposed to the coronavirus also died at a rate unparalleled in the general public. Criminal justice reform advocates pushed government to reduce the number of incarcerated people in order to protect the health of incarcerated individuals.
Successful efforts by criminal justice advocates were also effective public health measures that helped protect facility staff and surrounding communities because the failure to reduce the numbers of people in congregate settings also puts people in the community at risk. Although the higher infection and death rates among BIPOC and institutionalized individuals were often reported separately, advocates recognized that the outbreaks in both communities were interrelated. Because the vast majority of nursing facility staff working with residents are BIPOC, infections readily spread between the institutions and BIPOC communities, amplifying both outbreaks and killing BIPOC and institutionalized individuals at even greater rates.
In the face of the Delta variant (and other future variants), there is one critical thing that the Biden Administration needs to do to safeguard the lives of individuals in all congregate settings:
GET PEOPLE OUT!
For people with disabilities in institutional settings, the availability of community-based services has increased dramatically since Lois Curtis and Elaine Wilson took their fight for freedom all the way to the Supreme Court. Even so, Disabled individuals continue to be needlessly institutionalized. This was thoroughly documented in the 2013 Senate HELP Committee report, “Separate and Unequal: States Fail to Fulfill the Community Living Promise of the Americans with Disabilities Act” which called on Congress “to clarify and strengthen the law’s integration mandate in a manner that accelerates Olmstead implementation and clarifies that every individual who is eligible for LTSS under Medicaid has a federally protected right to a real choice in how they receive services and supports.”
The Biden Administration has limited its efforts addressing this issue by calling for increased funding for Home and Community Based Services (HCBS). Legislation has been put forward that would have the federal government entirely fund HCBS, however that legislation falls short in failing to ensure that elderly and Disabled individuals are no longer forced into institutional settings. For specific information, read the analysis from ADAPT.
Consequently, such efforts appear to be little more than a federal giveaway to providers who will provide the services and managed care companies that will manage the funds. The Biden proposals also focus on advancing the interests of the unions. By failing to give Disabled people the right to leave institutions, the Biden administration is protecting union jobs in the institutional settings. Efforts to expand HCBS seem more focused on advancing the interests of unions which organize in this sector – even when such efforts undermine the independence and freedom of people with disabilities as we are seeing in California right now. The Biden Administration needs to acknowledge the limitations of the Olmstead decision and publicly urge Congress to enact civil rights legislation addressing the injustice of unwanted institutionalization.
We cannot wait for Congress to take action; immediate action is needed. Using the full authority of the Centers for Medicare and Medicaid Services (CMS), the Biden Administration must ensure that states utilize the funds made available by Congress in response to the pandemic to support community integration programs and Home and Community Based Services which allow people to leave the institutions and support others in avoiding institutional placement.
Instead of ensuring that elderly and Disabled people can leave dangerous institutions, CMS has been giving states far too much latitude in how they use these funds. In one particularly egregious example, New York State is proposing to use the enhanced HCBS FMAP for worker retention in nursing facilities (see page 12) while refusing to raise the wages of personal care aides and consumer-directed personal assistants – even temporarily – in spite of the fact that such workers earn LESS than fast food workers in our state!
Additionally, Federal Emergency Management Agency (FEMA) funds should be made available to states to support efforts that allow nursing facility residents to leave the institution during the “pandemic emergency period” by providing transition support and – if necessary – supplemental personal assistance services and emergency housing. CDR attempted to work with Monroe County to do this early in the pandemic, but without federal or state support, the project went nowhere.
The time to act is now! Whether there is another new and even more virulent variant or immunity from the current vaccines wanes, we cannot wait to take action until residents in nursing facilities and other congregate settings begin dying. By then, as we saw during the early stages of the pandemic, any meaningful response will be too late to prevent needless deaths.
AND KEEP PEOPLE OUT!
Advocates for criminal justice reform effectively made the case for reducing the population of jails and prisons and have pressured the Biden administration to revoke a Trump-era Justice Department memo which said inmates whose sentences lasted beyond the “pandemic emergency period” would have to go back to prison. Unfortunately, the Biden administration has determined that thousands of individuals in federal prisons who were released to home confinement to reduce the risk of spreading COVID-19 will be required to return to prison after the pandemic’s official state of emergency ends.
President Biden – himself – has the power to address this. The President should use the power of clemency to commute the sentences of people living in home confinement. In fact, twenty organizations, including the American Civil Liberties Union, have written the Biden administration and urged them not to recall inmates from home confinement when the emergency ends. In part, their letter reads:
“President Biden, we ask that you use your power of clemency to commute the sentences of people living in home confinement due to the CARES Act and prevent this impending crisis. We ask that you issue an order that contains a presumption that all people in home confinement under the CARES Act will have their sentences commuted, unless the Bureau of Prisons can prove an articulable and current threat of violent harm.”
The disregard for these lives is appalling, but not surprising. Aside from being at greater risk of dying from COVID-19, incarcerated individuals and institutionalized elderly or disabled individuals have much more in common. Neither is represented in the main dataset of the US census, and both are seen as less-than-human. As we struggle to come out of the pandemic, we should not strive for getting back to what was “normal”, we should do better.
And to get us there we need a President who will lead us.